A single value of high-sensitive troponin T below the limit of detection is not enough for ruling out non ST elevation myocardial infarction in the emergency department

被引:8
作者
Chenevier-Gobeaux, Camille [1 ]
Meune, Christophe [2 ,3 ]
Lefevre, Guillaume [4 ]
Doumenc, Benoit [5 ,6 ]
Sorbets, Emmanuel [2 ,3 ]
Peschanski, Nicolas [7 ]
Ray, Patrick [7 ,8 ,9 ]
机构
[1] HUPC, Hop Cochin, AP HP, Dept Automated Biol Diag, F-75014 Paris, France
[2] Hop Univ Paris Seine St Denis, Hop Avicenne, AP HP, Dept Cardiol, Bobigny, France
[3] Univ Paris 13, UMR S 942, Paris, France
[4] HUEP, Hop Tenon, AP HP, Dept Biochem & Hormonol, 4 Rue Chine, F-75020 Paris, France
[5] HUPC, Hop Cochin, AP HP, Dept Emergency Med, F-75014 Paris, France
[6] Univ Paris 05, Paris, France
[7] HUEP, Hop Tenon, AP HP, Dept Emergency Med, 4 Rue Chine, F-75020 Paris, France
[8] Univ Paris 06, Sorbonne Univ, Paris, France
[9] Univ Paris 06, DHU Fighting Aging & Stress FAST, Paris, France
关键词
High sensitive troponin; Chest pain; Acute myocardial infarction; Emergency department; Acute coronary syndrome; CARDIAC TROPONIN; RULE-OUT; ASSAY; VALIDATION; DIAGNOSIS; ALGORITHM;
D O I
10.1016/j.clinbiochem.2016.05.021
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Recent 2015 ESC recommendations for the management of patients with suspected acute myocardial infarction (AMI) support that a single value of high-sensitivity cardiac troponin (HS-cTn) measured at presentation could rule out AMI if below the limit of blank (LoB) or detection (LoD). Objectives: We aimed to evaluate whether an undetectable HS-cTnT at presentation safely rules out NSTEMI in unselected patients with chest pain. Patients and methods: This is a post hoc analysis of two prospective cohorts with similar design that included patients suspected of AMI at three French university hospitals. Patients were followed-up during one month, before the adjudication of a final diagnosis. Results:413 patients (mean age 58 +/- 7 years) were analyzed; 45 (11%) had a final diagnosis of NSTEMI, and 26 (6%) had STEMI. The sensitivity of HS-cTnT value at 3 ng/L (LoB) for NSTEMI was 97.8% [95% CI: 86.8-99.9], yielding a negative predictive value (NPV) of 99.3% [95% CI: 95.4-100.0]. Proportion of patients ruled out for NSTEMI was 32% when applying the LoB. The sensitivity of HS-cTnT value at 5 ng/L (LoD) was 97.8% [95% CI: 86.8-99.9] yielding a NPV of 99.5% [95% CI: 96.5-100.0]. Proportion of patients ruled out for NSTEMI was 43% when applying the LoD. One patient (delay between onset of chest pain and presentation <3 h) had NSTEMI and HS-cTnT <LoB at presentation. Conclusion: The NPV of a single measurement of HS-cTnT below the LoD is high in unselected patients, but not enough to rule out safely NSTEMI for very early presenters. (C) 2016 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1113 / 1117
页数:5
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